A novel mutation (deletion of Aα-Asn 80) in an abnormal fibrinogen-Reference-Cited by-同舟云学术

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A novel mutation (deletion of Aα-Asn 80) in an abnormal fibrinogen

Published:2004-10 Issue:7 Volume:15 Page:559-567
ISSN:0957-5235
Container-title:Blood Coagulation & Fibrinolysis
language:en
Short-container-title:Blood Coagulation & Fibrinolysis

Author:

Marchi Rita C,Meyer Michael H,de Bosch Norma B,Arocha-Piñango C L,Weisel John W

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Hematology,General Medicine

Reference44 articles.

1. Dimeric half-molecules of human fibrinogen are joined through disulfide bonds in an antiparallel orientation

2. Disulfide bridges in NH2-terminal part of human fibrinogen

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1. The fibrin B?125-135 site is involved in the lateral association of protofibrils;The Ukrainian Biochemical Journal;2020-08-13

2. Structural Insights into Fibrinogen Dynamics Using Amide Hydrogen/Deuterium Exchange Mass Spectrometry;Biochemistry;2013-08-02

3. Fibrinogen Gdansk: Hypofibrinogenemia associated with a novel missense mutation in FGA (Ser112Pro);Thrombosis Research;2012-09

4. S-Nitrosoglutathione Acts as a Small Molecule Modulator of Human Fibrin Clot Architecture;PLoS ONE;2012-08-20

5. Comparison of the effect of different homocysteine concentrations on clot formation using human plasma and purified fibrinogen;Thrombosis and Haemostasis;2008

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